Label: CHARCOAL BLACKHEAD CLEARING SCRUB- salicylic acid cream
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-0910-28 - Packager: Walgreen Co
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated September 6, 2017
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- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
- Directions
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Inactive ingredients
water, sodium laureth sulfate, synthetic wax, sodium chloride, acrylates copolymer, coco-betaine, cocamide MEA, glycerin, charcoal powder, citric acid, polyglycerin-10, polyglyceryl-10 myristate, polyglyceryl-10 stearate, PPG-5-ceteth-20, sodium hydroxide, trisodium ethylenediamine disuccinate, fragrance, lecithin, red 40 lake, blue 1 lake, yellow 6 lake
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INGREDIENTS AND APPEARANCE
CHARCOAL BLACKHEAD CLEARING SCRUB
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0910 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20.6 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099) SODIUM CHLORIDE (UNII: 451W47IQ8X) CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L) COCO-BETAINE (UNII: 03DH2IZ3FY) COCO MONOETHANOLAMIDE (UNII: C80684146D) GLYCERIN (UNII: PDC6A3C0OX) ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POLYGLYCERIN-10 (UNII: P9060O936A) POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91) PPG-5-CETETH-20 (UNII: 4AAN25P8P4) SODIUM HYDROXIDE (UNII: 55X04QC32I) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0910-28 148 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/01/2016 Labeler - Walgreen Co (008965063) Registrant - Vi-Jon (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon 790752542 manufacture(0363-0910)